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Morphogenic regulator EFG1 affects the drug susceptibilities of pathogenic Candida albicans

机译:形态发生调节因子EFG1影响致病性白色念珠菌的药敏性

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This study shows that the morphogenic regulator EFG1 level affects the drug susceptibilities of Candida albicans when grown on solid growth media. The efg1 mutant showed sensitivity particularly to those drugs that target ergosterol or its metabolism. Efg1p disruption showed a gene-dosage effect on drug susceptibilities and resulted in enhanced susceptibility to drugs in the homozygous mutant as compared with the wild type, heterozygous and revertant strains. The enhanced sensitivity to drugs was independent of the status of ATP-binding cassette and MFS multidrug efflux pumps of C. albicans. The efg1 mutant displayed increased membrane fluidity that coincided with the downregulation of ERG11 and upregulation of OLE1 and ERG3, leading to enhanced passive diffusion of drugs. Interestingly, efg1 mutant cells displayed enhanced levels of endogenous ROS levels. Notably, the higher levels of ROS in the efg1 mutant could be reversed by the addition of antioxidants. However, the restoration of ROS levels did not reverse the drug sensitivities of the efg1 mutant. Taken together, we, for the first time, establish a new role to EFG1 in affecting the drug susceptibilities of C. albicans cells, independent of ROS and known drug efflux mechanisms.
机译:这项研究表明,当在固体生长培养基上生长时,形态发生调节因子EFG1水平会影响白色念珠菌的药敏性。 efg1突变体对那些针对麦角固醇或其代谢的药物特别敏感。与野生型,杂合性和回复性菌株相比,Efg1p破坏显示了对药物敏感性的基因剂量效应,并导致纯合突变体对药物的敏感性增强。对药物的敏感性增强与白色念珠菌的ATP结合盒和MFS多药外排泵的状态无关。 efg1突变体显示出增加的膜流动性,与ERG11的下调以及OLE1和ERG3的上调同时发生,从而导致药物的被动扩散增强。有趣的是,efg1突变细胞显示出增强的内源性ROS水平。值得注意的是,efg1突变体中较高水平的ROS可以通过添加抗氧化剂来逆转。但是,ROS水平的恢复并没有逆转efg1突变体的药物敏感性。总之,我们首次建立了EFG1在影响白色念珠菌细胞药敏性方面的新角色,而与ROS和已知的药物外排机制无关。

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